Phase 2 Lymphoma Trial, Recruiting NCT03125642 Sponsor: Masonic Cancer Center, University of Minnesota Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT03125642
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with Non-Hodgkin's Lymphoma (NHL) where the cancer has responded to chemotherapy, with eligibility depending on the specific type of NHL and how many treatment rounds have been completed (confirm with trial site for details on specific sub-types)
  • People who have been diagnosed with Hodgkin Lymphoma (HL) whose cancer has not been fully controlled by previous treatments, and whose disease has shown at least some response to chemotherapy
  • People with certain types of lymphoma who have high-risk features at diagnosis, such as advanced-stage disease or high levels of certain markers in the blood (confirm with trial site for full list of high-risk features)
  • People who are HIV-positive may still be considered, provided they have been assessed by an HIV/infectious disease specialist before joining, are on the most effective available HIV treatment, have a CD4+ cell count of at least 50 per microlitre, and have had a low HIV viral load (no more than 100,000 copies per mL) confirmed on two separate tests taken four weeks apart, with the most recent test within 30 days of enrolment
  • People with a performance status score of 80% or above on standard scales used for adults (aged 16 and over) or children (under 16), though a lower score may be accepted if poor health is caused by the lymphoma itself (confirm with trial site)
  • People whose blood counts, kidney function, liver function, heart function, and lung function all meet certain minimum levels as assessed by the treating team
  • People with a history of lymphoma involvement in the brain or spinal cord may be eligible for a specific treatment arm, provided they have completed standard treatment for this and show no signs of the disease progressing at the time of enrolment
  • People who are carriers of Hepatitis B (but not actively ill from it)
  • People who are at least four weeks past their last chemotherapy treatment (or six weeks if the treatment included a specific class of drugs called nitrosoureas)
  • People who are able and willing to use effective contraception for the duration of treatment, if there is any possibility of pregnancy
  • People who are able to give voluntary written consent to participate

Who may not be able to join:

  • People who are currently pregnant or breastfeeding — a blood or urine pregnancy test is required within 14 days before registration for anyone who could potentially become pregnant
  • People whose lymphoma has not responded to chemotherapy (chemotherapy-resistant disease)
  • People who are eligible for another transplant trial that has been given a higher priority
  • People who have an active, unrelated infection at the time of enrolment

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Veronika Bachanova, MD, Masonic Cancer Center, University of Minnesota

Phone: 612-273-2800

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Masonic Cancer Center, University of Minnesota
Registry
ClinicalTrials.gov
Start date
20 April 2017
Est. completion
30 September 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression Free Survival Comparison

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov